borofergie
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http://www.nature.com/nm/journal/vaop/ncurrent/full/nm.2414.html#/methodsMice were provided either a standard diet (16.4% protein, 73.1% carbohydrates and 10.5% fat with 4.07 kcal g−1; D12329, Research Diets) or a high-fat diet (16.4% protein, 25.5% carbohydrates and 58.0% fat with 5.56 kcal g−1; D12331, Research Diets).
And there could also be a chicken/egg situation where this same disrupted homeostasis leads to excess fat storage... a vicious cycle.RussG said:... the point seems to be that becoming obese interrupts the mechanism for glucose / insulin homeostasis, i.e. the counter regulatory effect of glucose and insulin production / reception ...
pianoman said:And there could also be a chicken/egg situation where this same disrupted homeostasis leads to excess fat storage... a vicious cycle.RussG said:... the point seems to be that becoming obese interrupts the mechanism for glucose / insulin homeostasis, i.e. the counter regulatory effect of glucose and insulin production / reception ...
The breakdown by macronutrients does not answer my question about the types of fats.
Science is supposed to be about generating questions.
Regarding the dietary breakdowns I think it important to be clear when referring to the percentage of energy from each macronutrient, that these diets were not isocaloric: with the standard diet at 4.07 kcal/gm and the high-fat at 5.56 kcal/gm... surely they deliberately overfed the high-fat mice? Which would mean changing multiple variables at the same time.Mice were provided either a standard diet (16.4% protein, 73.1% carbohydrates and 10.5% fat with 4.07 kcal g−1; D12329, Research Diets) or a high-fat diet (16.4% protein, 25.5% carbohydrates and 58.0% fat with 5.56 kcal g−1; D12331, Research Diets).
Surely if the cause is diet, then why reach for a patent-able and profitable solution rather than a simple dietary intervention?"The identification of the molecular players in this pathway to diabetes suggests new therapeutic targets and approaches towards developing an effective preventative or perhaps curative treatment. This may be accomplished by beta cell gene therapy or by drugs that interfere with this pathway in order to maintain normal beta cell function."
A connection between diet, obesity and diabetes exists in multiple species and is the basis of an escalating human health problem. The factors responsible provoke both insulin resistance and pancreatic beta cell dysfunction but remain to be fully identified. We report a combination of molecular events in human and mouse pancreatic beta cells, induced by elevated levels of free fatty acids or by administration of a high-fat diet with associated obesity, that comprise a pathogenic pathway to diabetes. Elevated concentrations of free fatty acids caused nuclear exclusion and reduced expression of the transcription factors FOXA2 and HNF1A in beta cells. This resulted in a deficit of GnT-4a glycosyltransferase expression in beta cells that produced signs of metabolic disease, including hyperglycemia, impaired glucose tolerance, hyperinsulinemia, hepatic steatosis and diminished insulin action in muscle and adipose tissues. Protection from disease was conferred by enforced beta cell–specific GnT-4a protein glycosylation and involved the maintenance of glucose transporter expression and the preservation of glucose transport. We observed that this pathogenic process was active in human islet cells obtained from donors with type 2 diabetes; thus, illuminating a pathway to disease implicated in the diet- and obesity-associated component of type 2 diabetes mellitus.
Elevated concentrations of free fatty acids caused nuclear exclusion and reduced expression of the transcription factors FOXA2 and HNF1A in beta cells. This resulted in a deficit of GnT-4a glycosyltransferase expression in beta cells that produced signs of metabolic disease, including hyperglycemia, impaired glucose tolerance, hyperinsulinemia, hepatic steatosis and diminished insulin action in muscle and adipose tissues. Protection from disease was conferred by enforced beta cell–specific GnT-4a protein glycosylation and involved the maintenance of glucose transporter expression and the preservation of glucose transport
Pianoman: Surely if the cause is diet, then why reach for a patent-able and profitable solution rather than a simple dietary intervention?
Not novel at all, so why do they continue to use trans fats in these trials knowing that they are harmful?. Not novel but not insignificant either... especially as this trial seems to pivot on FFAs which they suggest are due to a diet high in a type of fats for which many Doctors have called for an outright ban on human consumption. And although the detail breakdown of these diets was freely available for those of us savvy enough to dig down and use the internet, there is no mention of trans fats anywhere in the other papers or articles. That for me places a huge question mark over the integrity of this research.RussG said:I agree that the intake levels differed significantly - all that suggests though is that trans fats are not directly harmful in themselves, but they are in high quantities. I don't think that's particularly novel.
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